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CS-W001157 4
Total: USD 88.00

(S)-2-(N-Benzylprolyl)aminobenzophenone

  • CAS No. 96293-17-3

  • Cat. No. CS-0011031
  • Purity≥97%
  • MDL No.MFCD00145260

*For research and further manufacturing use only, not for direct human use.

(S)-2-(N-Benzylprolyl)aminobenzophenone|CS-0011031

Structure of 96293-17-3

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General Information

  • CAS No. 96293-17-3
  • Cat. No. CS-0011031
  • Purity ≥97%
  • MDL No. MFCD00145260
  • Storage RT, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₅H₂₄N₂O₂
  • Molecular Weight 384.47
  • Synonym(s) 2-Pyrrolidinecarboxamide, N-(2-benzoylphenyl)-1-(phenylmethyl)-, (S)-; (S)-N-(2-Benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide; (S)-2-[N'-(N-BENZYLPROLYL)AMINO]BENZOPHENONE
  • SMILES O=C(C1=CC=CC=C1)C2=CC=CC=C2NC([C@H]3N(CC4=CC=CC=C4)CCC3)=O

Description

This chiral scaffold integrates a benzylproline-derived amine with a benzophenone core, enabling asymmetric synthesis of bioactive compounds. The stereogenic center at the proline moiety ensures high enantioselectivity in catalytic transformations, while the aromatic ketone serves as a robust handle for further functionalization under standard conditions.

Application

(S)-2-(N-Benzylprolyl)aminobenzophenone serves as a chiral building block for synthesizing bioactive heterocycles and peptidomimetics. Its amine functionality enables straightforward derivatization, while the benzophenone core offers structural rigidity and π-stacking potential. The molecule exhibits bench stability and compatibility with standard coupling conditions, facilitating incorporation into complex scaffolds via amide bond formation or reductive amination.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   49.41
  • LogP   4.5207
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   6

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